Cervicouterine device that increases protection against the risk of contracting cervicouterine cancer

ABSTRACT

A uterine cervical device is provided whose antiviral properties of copper have been directed, broadened and extended to reduce the risk of contracting uterine cervical cancer and act as a preventive factor in cervical carcinogenesis. This is achieved by concentrating, increasing and distributing the copper adjacent the female reproductive apparatus, consisting of the lower part of the uterine cavity and the endocervix, an incubation site of the human papillomavirus, the leading cause of uterine cervical cancer. The device as presented increases the ionic capacity of copper by increasing its surface to 418 mm, and spacing out coils of the winding, incorporating a length of the same material, and positioning it directly in the cervix, which is shaped like a coil, Solomon Bar, bracelet or Celtic Knot, having assembled the copper filaments on a plastic frame of sizes that correspond to the proportions of the uterine cavity according to its parity.

BACKGROUND

Uterine cervical cancer is a public health problem worldwide, primarily affecting women in emerging countries, Mexico included.

German scientist Harald zur Hausen, awarded the Nobel Prize for Medicine in 2008, discovered the major role that the human papillomavirus has in the development of cervical cancer. ^([1])

In this country (Mexico), according to the Newscure study by Dr. Jose de Jesus Curiel, there are two million women infected with human papillomavirus: HPV and 600 000 have a premalignant lesion in the cervix^([2]). Moreover, the National Institute of Public Health, in the document entitled: Cuentas en Salud Reproductiva y Equidad de Género (Accounts in Reproductive Health and Gender Equality)^([3]) reported 4, 169 deaths from cervical-uterine cancer, i.e., one every two hours, more than ninety percent in women over 40 years of age. The reason for this rate of incidence is due to the fact that the virus requires many attempts to alter the cells and takes a long time to do so, which explains why infection is most common in the young and cancer is most common at older ages.

However, there is a contradiction whereby, although it is a pathology that is feasibly cured, if detected in early stages and treated in good time, there continues to be so many deaths, despite the existence of a vaccine, which does not provide complete protection and presents side effects that have led to the suspension of its application in several countries on this continent, in Europe and in Asia.

Moreover, there are efficient, reliable, safe alternatives which, based on extensive scientific studies like the one published in the prestigious scientific-medical journal Lancet Oncology in Great Britain in September 2011, comprising 26 epidemiological studies in eight countries, including Mexico, it was found that the presence of intrauterine devices with copper halved the risk of contracting uterine cervical cancer caused by the human papillomavirus and its ongoing protective effect remains significant for 10 years.^([4])

In turn, the US Environment Protection Agency (EPA), alarmed by the high mortality caused by nosocomial infections, sponsored a study whereby the bactericidal, fungicidal and antiviral properties of copper were corroborated, since in the space of two hours, it kills 99.9% of these, including Staphylococcus aureus that is resistant to methicillin, an antibiotic being used to combat super-bacteria.^([5])

It has also proven effective against Candida A, which causes vaginitis in Mexican women; and many others, such as the H1N1 influenza virus, adenovirus, E. coli 0157 Clostridium difficile, etc.^([6])

In Mexico, uterine cervical cancer is the leading cause of neoplasms in women over 25 years. This scourge mainly affects women on low incomes, in places with little or no access to health services, located across countless small, scattered and hard-to-reach localities. There are 10 million people living in 170, 000 localities with less than 500 inhabitants who have scarcely any possibility of being reached by the official programs for early detection through the application of the Papanicolaou test, which often detects very advanced cases of uterine cervical cancer. ^([7])

As with all public health problems, the solution lies in their prevention. In this area, the 380 A copper-T intrauterine device has played an important preventive role, because in its standard presentation it has been able to reduce the risk of cervical cancer by 50%, even though, despite its dimensions, currently only 7% of women of childbearing age use it due to dimensional incompatibility. ^([8, 9, 10])

The answer is offered by the uterine cervical device that presents technical innovations consisting, inter alia, of increased copper 418 mm ions.

The present invention develops a preventive method to avoid the transformation of the human papillomavirus into cervical cancer, causing its preventive effects in the region of the female reproductive organs, particularly opposite the cavities that make up the endocervix, significantly reducing this scourge, regardless of accessibility to institutions and affordability

PRIOR ART

The present invention relates to intrauterine devices; it is a substantial improvement related to patent MX213004 DISPOSITIVO INTRAUTERINO T DE COBRE CORTO PARA NULIPARAS MUJERES Y/O BREVILINEAS that protects a contraceptive method.

A uterine cervical device is also known, as described in patent CN102369003 (A) INTRA-CERVICAL DEVICE FOR THE LOCAL RELEASE OF DRUGS IN THE LOCAL-REGIONAL TREATMENT OF CERVICAL CANCER, for local delivery of drugs for the treatment of tumors of the cervix.

There is also a “vaccine” that protects against some types of human papillomavirus. The United States Food and Drug Administration (FDA) has approved two presentations of it.

DESCRIPTION

The present invention describes a uterine cervical device that increases protection against the development of uterine cervical cancer caused mainly by the human papillomavirus, leveraging the antiviral properties of copper by increasing, regrouping and redistributing the copper surface, and its concentration to 82% in the most vulnerable region of the female reproductive system. It consists of a frame of inert plastic such as low-density polyethylene, polypropylene, Dacron or Silastic in a T-shape (FIG. 1 (A, B)) into which is incorporated between 15% and 23% radiopaque barium sulfate and titanium oxide as a dye.

A first innovation consists in the increase and concentration of 418 mm² of copper as well as its redistribution in the manner detailed in FIG. (1)

A second innovation is that the horizontal arm of the frame (A) has a length between 18.0±2 mm and 32.0±2 mm and a diameter of 1.7 mm on which is wound or coiled a 0.25-0.26 mm strand of copper (C) each of 36 mm² to give a total of 72.0±2 mm² forming an aerodynamic shape during the insertion process that eliminates the sharp edge caused by the angle of the cylinders of the same material.

A third innovation is that the vertical post or arm (B), which has 26.0±2 mm and 36.0±2 mm at its lower end has 200 mm² of copper filament in two layers wound or coiled on it, each with 100 mm² and 123 mm in length each totaling 200 mm² (D).

A fourth innovation is the 0.30 mm spaced pitch of the coils (E) which allows double the release of copper ions over the usual winding. The distance of the double winding and the accent of the frame, is between 20.0 and 25.0 mm.

A fifth innovation is that the vertical post or arm has, at its final end a sphere made of plastic and/or copper measuring 3.1 mm in diameter (F).

A sixth innovation is that, within the area of the sphere (G) are located the ends of a length of 99.9% pure copper, oxygen-free winding with a length of between 150 and 300 mm and 146-250 mm², placed on the uterine cervical canal right opposite the folds or cavities of the cervix, where the human papillomaviruses are incubated, with the possibility that both the length and mm² of the copper surface may vary, without exceeding the measurements of the cervix or the total 418 mm² of the total copper surface in uterine cervical device (G).

A seventh innovation is that length can have different shapes, such as a Solomon Bar, Celtic Knot, Bracelet (H, I, J).

The eighth innovation consists of various measurements of the frame that are contained in FIG. (1) in order to achieve the proper operation and tolerance of the uterine cervical device inside the uterine cavity.

The ninth innovation, consists of a plunger or piston which has a recess at its final end to lodge the extension of the uterine cervical device into the cervical canal. (FIG. 8)

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 Frontal View of a plastic T-shaped frame which is 1.7 mm in diameter and has the following measurements: Horizontal arm 18.0±2 mm-32.0±2 mm in length (A): the vertical post measures 26.0±2 mm-36.0±2 mm (B) and at its lower end it has a plastic or copper sphere with a diameter of 3.1 mm (F). Wound on each side of the horizontal arm is a strand of copper each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm² (C). At the bottom of the vertical post are wound two superimposed filament layers of copper each with 100 mm² of copper with a total of 200 mm² (D) and whose coils are spaced at 0.30 mm (E). Inside the sphere are placed the ends of a length of coiled copper wire or Solomon Bar,

Celtic Knot or Bracelet with 146 mm² to 250 mm² (G) totaling a 418-mm² area of copper.

Nulligravida FIG. 2 Frontal View of a plastic T-shaped frame which is 1.7 mm in diameter and has the following measurements: Horizontal arm 18.0±2 mm in length (A): the vertical post measures 26.0±2 mm (B) and at its lower end it has a plastic or copper sphere with a diameter of 3.1 mm (F). Wound on each side of the horizontal arm is a strand of copper measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm² each, totaling 72.0±2 mm² (C). At the bottom of the vertical post are wound two superimposed filament layers of copper each with 100 mm² of copper with a total of 200 mm² (D) and whose coils are spaced at 0.30 mm (E). Inside the sphere are placed the ends of a length of coiled copper wire or Solomon Bar, Celtic Knot or Bracelet with 146 mm² to 250 mm² (G) totaling a 418-mm² area of copper.

Nullipara: FIG. 3.

Frontal View of a plastic T-shaped frame which is 1.7 mm in diameter and has the following measurements: Horizontal arm 22.0±2 mm in length (A): the vertical post measures 28.0±2 mm (B) and at its lower end it has a plastic or copper sphere with a diameter of 3.1 mm (F).

Wound on each side of the horizontal arm is a strand of copper each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm² (C). At the bottom of the vertical post are wound two superimposed filament layers of copper each with 100 mm² of copper with a total of 200 mm² (D) and whose coils are spaced at 0.30 mm (E). Inside the sphere are placed the ends of a length of coiled copper wire or Solomon Bar, Celtic Knot or Bracelet with 146 mm² to 250 mm² (G) totaling a 418-mm² area of copper.

Parity 1 FIG. 4

Frontal View of a plastic T-shaped frame which is 1.7 mm in diameter and has the following measurements: Horizontal arm 24.0±2 mm in length (A): the vertical post measures 30.0 ±2 mm (B) and at its lower end it has a plastic or copper sphere with a diameter of 3.1 mm (F). Wound on each side of the horizontal arm is a strand of copper each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm² (C). At the bottom of the vertical post are wound two superimposed filament layers of copper each with 100 mm² of copper with a total of 200 mm² (D) and whose coils are spaced at 0.30 mm (E). Inside the sphere are placed the ends of a length of coiled copper wire or Solomon Bar, Celtic Knot or Bracelet with 146 mm² to 250 mm² (G) totaling a 418-mm² area of copper.

Parity 2 FIG. 5

Frontal View of a plastic T-shaped frame which is 1.7 mm in diameter and has the following measurements: Horizontal arm 26.0±2 mm in length (A): the vertical post measures 32.0±2 mm (B) and at its lower end it has a plastic or copper sphere with a diameter of 3.1 mm (F). Wound on each side of the horizontal arm is a strand of copper each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm² (C). At the bottom of the vertical post are wound two superimposed filament layers of copper each with 100 mm² of copper with a total of 200 mm² (D) and whose coils are spaced at 0.30 mm (E). Inside the sphere are placed the ends of a length of coiled copper wire or Solomon Bar, Celtic Knot or Bracelet with 146 mm² to 250 mm² (G) totaling a 418-mm² area of copper.

Parity 3 FIG. 6 Frontal View of a plastic T-shaped frame which is 1.7 mm in diameter and has the following measurements: Horizontal arm 28.0±2 mm in length (A): the vertical post measures 34.0±2 mm (B) and at its lower end it has a plastic or copper sphere with a diameter of 3.1 mm (F). Wound on each side of the horizontal arm is a strand of copper each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm² (C). At the bottom of the vertical post are wound two superimposed filament layers of copper each with 100 mm² of copper with a total of 200 mm² (D) and whose coils are spaced at 0.30 mm (E). Inside the sphere are placed the ends of a length of coiled copper wire or Solomon Bar, Celtic Knot or Bracelet with 146 mm² to 250 mm² (G) totaling a 418-mm² area of copper.

Parity 4 or more FIG. 7 Frontal View of a plastic T-shaped frame which is 1.7 mm in diameter and has the following measurements: Horizontal arm 32.0±2 mm in length (A): the vertical post measures 36.0±2 mm (B) and at its lower end it has a plastic or copper sphere with a diameter of 3.1 mm (F). Wound on each side of the horizontal arm is a strand of copper each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm² (C). At the bottom of the vertical post are wound two superimposed filament layers of copper each with 100 mm² of copper with a total of 200 mm² (D) and whose coils are spaced at 0.30 mm (E).

Inside the sphere are placed the ends of a length of coiled copper wire or Solomon Bar, Celtic Knot or Bracelet with 146 mm² to 250 mm² (G) totaling a 418-mm² area of copper.

FIG. 8 Plunger

Front view of a plastic, piston-shaped device with a length (K) of 188-193 mm, on one of its ends in cylindrical space (L) with a length of 10 mm, lower diameter (M) 2.5 mm, outer diameter (N) 3.3 mm and the other end is shaped like a handle or grip (R).

BIBLIOGRAPHICAL REFERENCES

-   1. Zur Hausen H, 1996: Papillomavirus infections—A major cause of     human cancers. Biochim. Biophys Acta 1288:55-78 -   2. Virus delPapiloman Humano     Dr. José de Jésus Curiel

Newscure

-   3. Cuentas en Salud Reproductiva y Equidad de Genero

Primera Edición 2011 Instituto Nacional de Salud Pública

-   4. Intrauterine device use, cervical infection with human     papillomavirus, and risk of cervical cancer: a pooled analysis of 26     epidemiological studies.     Xavier Castellsague, Mireña Diaz, Salvatore Vaccarelia, Silvia de     Sanjose. Nubia Muñoz, Rolando Herrero, Silvia Franceschi. Chris M     Meijer. Et al. Intrauterine device use, cervical infection with     human papillomavirus, and risk of cervical cancer a pooled analysis     of 26 epidemiological studies Lancet Oncol. 2011 Oct. 12;     (11):1023-1031. -   5. REREGISTRATION ELIGIBILITY DECISION FOR COPPERS

Case Nos. 0636, 0649, 4025, 4026 Debra Edwards, Ph.D. Director, Special Review and Reregistration Division EPA

-   6. Cu Copper Development Association

International Copper Association Mexico Copper Alliance

-   7. El Cáncer Cervicouterino, su Impacto en México y el por qué no     funciona el programa nacional de Detección Oportuna.

Ana C. Hidalgo Martínez

Centro de Investigación sobre enfermedades Infecciosas Instituto Nacional de Salud Pública.

RevBiomed 2006 17;81-84

-   8. ABORTO CLANDESTINO

The Alan Guttmacher Institute N. Rutenber, M. Ayad.L.H.Ochoa and M. Wilkinson, “Knowledge and Use of Contraception”, DHS Comparative Studies, No.6, Julio de 1991, Cuadro 4.1;

And special analyses of Demographic and Health Surveys by the AGI

-   9. Reynoso L, Zamora G, Giner J, Gonzalez M., y Aznar R., Medidas de     la Cavidad uterina en mujeres mexicanas, Ginec. Obstet, Mex. J. Vol     45 Year XXXIV, No. 271, May 1979. -   10. Reynoso L, Zamora G., Gonzalez, Diddi M., Lozano M., Aznar R.,     <<Uterine metrology in<<Mexican women>>, in <<Biomedial Aspects of     IUDs>>, pp 119-124, published in the UK and Europe by Mtp. Press,     Lancaster England RG 137 ISBN 085200, 1982

REFERENCES Descriptive Notes

-   1. Coils: synonym helix: helicoidal; curve: curved, arched; bent;     convex; concave. -   2. ContracepFertil Sex. 1998 Nov;26 (11):781-9.     [Atomic absorption spectrophotometry study of copper ion released by     copper-bearing intrauterine devices].

Berthou J1, Chretien F C, Driguez P A.

Author information

-   3. Los iones y la Salud

El Ediciones by 2002 Argentina.

-   4. Manual de nudosmarinos.     http://www.marina.mil.pa.static.fHes -   5. Invasive Cervical Cancer and Intrauterine Device USE     International Journal of Epidemiology

©International Epidemiological Association 1991

DEBORAH L LASSISE***. DAVID A SAVITZ'f. RICHARD F HA MMAN*. ANNA E BARON*, LOUISE A BRINTONt AND ROBERTS LEVINES

-   6. REREGISTRATION ELIGIBILITY DECISION FOR COPPERS

Case Nos. 0636, 0649, 4025, 4026 Debra Edwards, Ph.D. Director, Special Review and Reregistration Division EPA

-   7. Cu Copper Development Association

International Copper Association Mexico Copper Alliance

-   8. Intrauterine device use, cervical infection with human     papillomavirus, and risk of cervical cancer: a pooled analysis of 26     epidemiological studies.     Xavier Castellsague, Mirena Diaz, Salvatore Vaccarelia, Silvia de     Sanjose. Nubia Munoz, Rolando Herrero, Silvia Franceschi. Chris M     Meijer. Et al. Intrauterine device use, cervical infection with     human papillomavirus, and risk of cervical cancer a pooled analysis     of 26 epidemiological studies Lancet Oncol. 2011 Oct. 12;     (11):1023-1031. -   9. Cuentas en Salud Reproductiva y Equidad de Genero Estimación     2009, Comparativo 2003-2009 Gobierno Federal. Instituto Nacional de     Salud Pública Mexico 2011

Explanatory Annex

-   1. Radiopacante. Medio de contraste positivo más utilizado sulfato     de bario y compuestos yodados: Ba S04     Medios de contraste en imagenologia

Agustina Chavez Sanchez May 17, 2013

-   2. Coils: synonym helix: helicoidal; curve: curved, arched; bent;     convex; concave. -   3. Contracept. Fertil Sex. 1998 Nov; 26 (11): 781-9     [Atomic absorption spectrophotometry study of copper ion release by     copper-bearing intrauterine devices].

Berthou J1, Chretien F C, Driguez P A.

Author information

-   4. Los iones y la Salud

El Ediciones by 2002 Argentina.

-   5. Manual de nudosmarinos.     http://www.marina.mil.pa.static.files 

1. Uterine cervical device that increases protection against the risk of contracting uterine cervical cancer caused mainly by the human papillomavirus in which it comprises the use and concentration of copper as an antiviral, having increased this element to 418 mm², distributed on a T-shaped frame, made of inert plastic such as low-density polyethylene, polypropylene, Dacron or Silastic, into which is incorporated between 15 and 23% radiopaque barium sulfate and titanium oxide as a colorant, concentrating 82% of the antiviral activity of this element in the region of the female reproductive system located at the lower part of the uterine cavity and endocervix where the human papillomavirus is incubated, the device comprises a horizontal tilde or arm (A) between 18.0±2 mm and 32.0±2 mm in length, on the vertical post or arm (B) between 26.0±2 mm and 36.0±2 mm in length and 1.7 mm in diameter, and a sphere (F) of the same material and/or of copper measuring 3.1 mm diameter; wound on each side of the horizontal arm (A) is a strand of copper (C) each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm²; wound on the vertical post or arm (B) are two overlapping copper filaments (D) each measuring 0.25-0.26 mm in diameter and 100 mm²; the distance of the double winding and the tilde is 20.0-25.0 mm, each one spaced (E) 0.30 mm apart, and (there is) a length of copper filament (G) of between 146 and 250 mm² wound or in the shape of a Solomon Bar, Celtic knot or bracelet (H, I, J), located opposite the cavities of the endocervix, which is the incubation site of the human papillomavirus, with the possibility of varying both the amount of mm² of copper surface without exceeding the measurements of the cervix or the 418 mm² of copper; inside the length is placed a thread or filament of low-density polyethylene with a length of 20 cm and diameter of 0.20-0.30 mm.
 2. Uterine cervical device that increases protection against the risk of contracting uterine cervical cancer caused mainly by the human papillomavirus according to claim 1, in which it comprises the use and concentration of copper as an antiviral, having increased this element to 418 mm², distributed on a T-shaped frame, made of inert plastic such as low-density polyethylene, polypropylene, Dacron or Silastic, into which is incorporated between 15 and 23% radiopaque barium sulfate and titanium oxide as a colorant, concentrating 82% of the antiviral activity of this element in the region of the female reproductive system located at the lower part of the uterine cavity and endocervix where the human papillomavirus is incubated; it. comprises a horizontal tilde or arm (A) 18.0±2 mm in length, on the vertical post or arm (B) 26.0±2 mm in length and 1.7 mm in diameter, and a sphere (F) of the same material and/or of copper measuring 3.1 mm diameter, wound on each side of the horizontal arm (A) is a strand of copper (C) each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm²; wound on the vertical post or arm (B) are two overlapping copper filaments (D) each measuring 0.25-0.26 mm in diameter and 100 mm². The the distance of the double winding and the tilde is 20.0-25.0 mm, each one spaced (E) 0.30 mm apart, and (there is) a length of copper filament (G) of between 146 and 250 mm² wound or in the shape of a Solomon Bar, Celtic knot or bracelet (H, I, J), located opposite the cavities of the endocervix, which is the incubation site of the human papillomavirus, with the possibility of varying both the amount of mm² of copper surface without exceeding the measurements of the cervix or the 418 mm² of copper; inside the length is placed a thread or filament of low-density polyethylene with a length of 20 cm and diameter of 0.20-0.30 mm.
 3. Uterine cervical device that increases protection against the risk of contracting uterine cervical cancer caused mainly by the human papillomavirus according to claim 1, in which it comprises the use and concentration of copper as an antiviral, having increased this element to 418 mm², distributed on a T-shaped frame, made of inert plastic such as low-density polyethylene, polypropylene, Dacron or Silastic, into which is incorporated between 15 and 23% radiopaque barium sulfate and titanium oxide as a colorant, concentrating 82% of the antiviral activity of this element in the region of the female reproductive system located at the lower part of the uterine cavity and endocervix where the human papillomavirus is incubated; the device comprises a horizontal tilde or arm (A) 22.0±2 mm in length, on the vertical post or arm (B) 28.0±2 mm in length and 1.7 mm in diameter, and a sphere (F) of the same material and/or of copper measuring 3.1 mm diameter; wound on each side of the horizontal arm (A) is a strand of copper (C) each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm²; wound on the vertical post or arm (B) are two overlapping copper filaments (D) each measuring 0.25-0.26 mm in diameter and 100 mm² the distance of the double winding and the tilde is 20.0-25.0 mm, each one spaced (E) 0.30 mm apart, and (there is) a length of copper filament (G) of between 146 and 250 mm² wound or in the shape of a Solomon Bar, Celtic knot or bracelet (H, I, J), located opposite the cavities of the endocervix, which is the incubation site of the human papillomavirus, with the possibility of varying both the amount of mm² of copper surface without exceeding the measurements of the cervix or the 418 mm² of copper; inside the length is placed a thread or filament of low-density polyethylene with a length of 20 cm and diameter of 0.20-0.30 mm.
 4. Uterine cervical device that increases protection against the risk of contracting uterine cervical cancer caused mainly by the human papillomavirus according to claim 1, in which it comprises the use and concentration of copper as an antiviral, having increased this element to 418 mm², distributed on a T-shaped frame, made of inert plastic such as low-density polyethylene, polypropylene, Dacron or Silastic, into which is incorporated between 15 and 23% radiopaque barium sulfate and titanium oxide as a colorant, concentrating 82% of the antiviral activity of this element in the region of the female reproductive system located at the lower part of the uterine cavity and endocervix where the human papillomavirus is incubated; the device comprises a horizontal tilde or arm (A) 24.0±2 mm in length, on the vertical post or arm (B) 30.0±2 mm in length and 1.7 mm in diameter, and a sphere (F) of the same material and/or of copper measuring 3.1 mm diameter; wound on each side of the horizontal arm (A) is a strand of copper (C) each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm²; wound on the vertical post or arm (B) are two overlapping copper filaments (D) each measuring 0.25-0.26 mm in diameter and 100 mm² the distance of the double winding and the tilde is 20.0-25.0 mm, each one spaced (E) 0.30 mm apart, and (there is) a length of copper filament (G) of between 146 and 250 mm² wound or in the shape of a Solomon Bar, Celtic knot or bracelet (H, I, J), located opposite the cavities of the endocervix, which is the incubation site of the human papillomavirus, with the possibility of varying both the amount of mm² of copper surface without exceeding the measurements of the cervix or the 418 mm² of copper; inside the length is placed a thread or filament of low-density polyethylene with a length of 20 cm and diameter of 0.20-0.30 mm.
 5. Uterine cervical device that increases protection against the risk of contracting uterine cervical cancer caused mainly by the human papillomavirus according to claim 1, in which it comprises the use and concentration of copper as an antiviral, having increased this element to 418 mm², distributed on a T-shaped frame, made of inert plastic such as low-density polyethylene, polypropylene, Dacron or Silastic, into which is incorporated between 15 and 23% radiopaque barium sulfate and titanium oxide as a colorant, concentrating 82% of the antiviral activity of this element in the region of the female reproductive system located at the lower part of the uterine cavity and endocervix where the human papillomavirus is incubated; the device comprises a horizontal tilde or arm (A) 26.0±2 mm in length, on the vertical post or arm (B) 32.0±2 mm in length and 1.7 mm in diameter, and a sphere (F) of the same material and/or of copper measuring 3.1 mm diameter; wound on each side of the horizontal arm (A) is a strand of copper (C) each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm²; wound on the vertical post or arm (B) are two overlapping copper filaments (D) each measuring 0.25-0.26 mm in diameter and 100 mm² the distance of the double winding and the tilde is 20.0-25.0 mm, each one spaced (E) 0.30 mm apart, and (there is) a length of copper filament (G) of between 146 and 250 mm² wound or in the shape of a Solomon Bar, Celtic knot or bracelet (H, I, J), located opposite the cavities of the endocervix, which is the incubation site of the human papillomavirus, with the possibility of varying both the amount of mm² of copper surface without exceeding the measurements of the cervix or the 418 mm² of copper; inside the length is placed a thread or filament of low-density polyethylene with a length of 20 cm and diameter of 0.20-0.30 mm.
 6. Uterine cervical device that increases protection against the risk of contracting uterine cervical cancer caused mainly by the human papillomavirus according to claim 1, in which it comprises the use and concentration of copper as an antiviral, having increased this element to 418 mm², distributed on a T-shaped frame, made of inert plastic such as low-density polyethylene, polypropylene, Dacron or Silastic, into which is incorporated between 15 and 23% radiopaque barium sulfate and titanium oxide as a colorant, concentrating 82% of the antiviral activity of this element in the region of the female reproductive system located at the lower part of the uterine cavity and endocervix where the human papillomavirus is incubated; the device comprises a horizontal tilde or arm (A) 28.0±2 mm in length, on the vertical post or arm (B) 34.0±2 mm in length and 1.7 mm in diameter, and a sphere (F) of the same material and/or of copper measuring 3.1 mm diameter; wound on each side of the horizontal arm (A) is a strand of copper (C) each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm²; wound on the vertical post or arm (B) are two overlapping copper filaments (D) each measuring 0.25-0.26 mm in diameter and 100 mm² the distance of the double winding and the tilde is 20.0-25.0 mm, each one spaced (E) 0.30 mm apart, and (there is) a length of copper filament (G) of between 146 and 250 mm² wound or in the shape of a Solomon Bar, Celtic knot or bracelet (H, I, J), located opposite the cavities of the endocervix, which is the incubation site of the human papillomavirus, with the possibility of varying both the amount of mm² of copper surface without exceeding the measurements of the cervix or the 418 mm² of copper; inside the length is placed a thread or filament of low-density polyethylene with a length of 20 cm and diameter of 0.20-0.30 mm.
 7. Uterine cervical device that increases protection against the risk of contracting uterine cervical cancer caused mainly by the human papillomavirus according to claim 1, in which it comprises the use and concentration of copper as an antiviral, having increased this element to 418 mm², distributed on a T-shaped frame, made of inert plastic such as low-density polyethylene, polypropylene, Dacron or Silastic, into which is incorporated between 15 and 23% radiopaque barium sulfate and titanium oxide as a colorant in a T-shape, concentrating 82% of the antiviral activity of this element in the region of the female reproductive system located at the lower part of the uterine cavity and endocervix where the human papillomavirus is incubated the device comprises a horizontal tilde or arm (A) 32.0±2 mm in length, on the vertical post or arm (B) 36.0±2 mm in length and 1.7 mm in diameter, and a sphere (F) of the same material and/or of copper measuring 3.1 mm diameter; wound on each side of the horizontal arm (A) is a strand of copper (C) each measuring 0.25 mm to 0.26 mm in diameter and 36.0±2 mm², totaling 72.0±2 mm²; wound on the vertical post or arm (B) are two overlapping copper filaments (D) each measuring 0.25-0.26 mm in diameter and 100 mm² the distance of the double winding and the tilde is 20.0-25.0 mm, each one spaced (E) 0.30 mm apart, and (there is) a length of copper filament (G) of between 146 and 250 mm² wound or in the shape of a Solomon Bar, Celtic knot or bracelet (H, I, J), located opposite the cavities of the endocervix, which is the incubation site of the human papillomavirus, with the possibility of varying both the amount of mm² of copper surface without exceeding the measurements of the cervix or the 418 mm² of copper; inside the length is placed a thread or filament of low-density polyethylene with a length of 20 cm and diameter of 0.20-0.30 mm.
 8. Uterine cervical device that increases protection against the risk of uterine cervical cancer caused mainly by human papillomavirus according to claim 1, in which there is an inserting plunger, with a length of 188-193 mm comprised of aplastic frame whose cylindrical end houses a 2-cm long recess with a 2.5-mm inner diameter and an outer diameter of 3.3 mm to accommodate the length of the uterine cervical device. 